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1-ACETYL-7-BROMO-5-IODOINDOLINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100034-32-0

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100034-32-0 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of 1-ACETYL-7-BROMO-5-IODOINDOLINE.

Explanation

1-ACETYL-7-BROMO-5-IODOINDOLINE is derived from indoline, which is a heterocyclic compound containing a six-membered ring with nitrogen.

Explanation

The compound has a bromine atom attached to the 7th position and an iodine atom attached to the 5th position, making it a halogenated indoline.

Explanation

1-ACETYL-7-BROMO-5-IODOINDOLINE is primarily used as a starting material for the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.

Explanation

The specific properties and applications of 1-ACETYL-7-BROMO-5-IODOINDOLINE are determined by the chemical reactions it undergoes and the desired end product.

Explanation

Due to its structure and reactivity, 1-ACETYL-7-BROMO-5-IODOINDOLINE can be used as a building block for the development of new pharmaceutical compounds.

Explanation

The compound can also be utilized in the synthesis of various agrochemicals, such as pesticides and herbicides, due to its versatile structure and reactivity.

Explanation

The presence of bromine and iodine atoms in the compound can affect its reactivity, making it suitable for specific chemical reactions and applications.

Explanation

The compound's structure consists of a six-membered ring with nitrogen, an acetyl group attached to the 1st position, and halogen atoms (bromine and iodine) attached to the 7th and 5th positions, respectively.

Derivative of Indoline

Yes

Halogenated Indoline

Yes

Acetyl Group Attachment

1st position

Main Use

Building block for organic synthesis

Specific Properties

Depend on chemical reactions and target compounds

Pharmaceutical Applications

Potential use in drug synthesis

Agrochemical Applications

Potential use in agrochemical synthesis

Reactivity

Influenced by bromine and iodine atoms

Structural Features

Six-membered ring with nitrogen, acetyl group, and halogen atoms

Check Digit Verification of cas no

The CAS Registry Mumber 100034-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,3 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100034-32:
(8*1)+(7*0)+(6*0)+(5*0)+(4*3)+(3*4)+(2*3)+(1*2)=40
40 % 10 = 0
So 100034-32-0 is a valid CAS Registry Number.

100034-32-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-benzylamino-2',3'-O-isopropylideneguanosine

1.2 Other means of identification

Product number -
Other names 2-Amino-8-benzylamino-9-((3aR,4R,6R,6aR)-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:100034-32-0 SDS

100034-32-0Relevant academic research and scientific papers

Systematic General Synthesis of Purine 8,5'-Imino and Substituted Imino Cyclonucleosides

Minamoto, Katsumaro,Fujiki, Yasumi,Shiomi, Niro,Uda, Yoriaki,Sasaki, Tadashi

, p. 2337 - 2346 (2007/10/02)

2',3'-O-Isopropylidene-8-methylaminoadenosine (7a), its hypoxanthine analogue (7b), 2',3'-O-isopropylidene-8-benzylaminoadenosine (7c), its hypoxanthine analogue (7d), 2',3'-O-isopropylidene-8-allylaminoadenosine (7e), its hypoxanthine analogue (7f), 8-be

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